The potential predictive value of DEK expression for neoadjuvant chemoradiotherapy response in locally advanced rectal cancer

被引:14
|
作者
Martinez-Useros, J. [1 ]
Moreno, I. [1 ]
Fernandez-Acenero, M. J. [2 ]
Rodriguez-Remirez, M. [1 ]
Borrero-Palacios, A. [1 ]
Cebrian, A. [1 ]
del Pulgar, T. Gomez [1 ]
del Puerto-Nevado, L. [1 ]
Li, W. [1 ]
Puime-Otin, A. [3 ]
Perez, N. [3 ]
Soengas, M. S. [4 ]
Garcia-Foncillas, J. [1 ]
机构
[1] Univ Hosp Fdn Jimenez Diaz UAM, Hlth Res Inst, OncoHlth Inst, Translat Oncol Div, Av Reyes Catolicos 2, Madrid 28040, Spain
[2] Clin San Carlos Univ Hosp, Dept Pathol, Madrid, Spain
[3] Univ Hosp Fdn Jimenez Diaz UAM, Dept Pathol, Madrid, Spain
[4] Spanish Natl Canc Res Ctr, Melanoma Res Grp, Madrid, Spain
关键词
DEK; Chemoradiotherapy; Neoadjuvant treatment; Rectal cancer; Predictive biomarker; Complete pathological response; TOTAL MESORECTAL EXCISION; PREOPERATIVE CHEMORADIOTHERAPY; PATHOLOGICAL RESPONSE; OVEREXPRESSION; IDENTIFICATION; THERAPY; GENES; P38; PROLIFERATION; RADIOTHERAPY;
D O I
10.1186/s12885-018-4048-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Limited data are available regarding the ability of biomarkers to predict complete pathological response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer. Complete response translates to better patient survival. DEK is a transcription factor involved not only in development and progression of different types of cancer, but is also associated with treatment response. This study aims to analyze the role of DEK in complete pathological response following chemoradiotherapy for locally advanced rectal cancer. Methods: Pre-treated tumour samples from 74 locally advanced rectal-cancer patients who received chemoradiation therapy prior to total mesorectal excision were recruited for construction of a tissue microarray. DEK immunoreactivity from all samples was quantified by immunohistochemistry. Then, association between positive stained tumour cells and pathologic response to neoadjuvant treatment was measured to determine optimal predictive power. Results: DEK expression was limited to tumour cells located in the rectum. Interestingly, high percentage of tumour cells with DEK positiveness was statistically associated with complete pathological response to neoadjuvant treatment based on radiotherapy and fluoropyrimidine-based chemotherapy and a marked trend toward significance between DEK positiveness and absence of treatment toxicity. Further analysis revealed an association between DEK and the pro-apoptotic factor P38 in the pre-treated rectal cancer biopsies. Conclusions: These data suggest DEK as a potential biomarker of complete pathological response to treatment in locally advanced rectal cancer.
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页数:11
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